• Studies of pH]5 HT release in vitro supports the suggestion the 5 HTib receptor, but not the 5 HTia somatodendritic autoreceptor, regulates evoked 5 HT release in raphe slices. (gabasignaling.com)
  • It has been shown, employing in vivo voltammetry, that GR127935 enhances although the 5 HTid receptor agonist, sumatriptan, inhibits the electrically evoked release buy Apatinib of 5 HT during the raphe in vitro, steady together with the existence of inhibitory 5 HTid autoreceptors inside of this framework. (gabasignaling.com)
  • It has been proposed that the inhibitory role of 5-HT 1A and 5-HT 1B serotonergic receptor sub-types that limit somatodendritic and nerve terminal 5-HT release, respectively, plays a key role in the mechanism of action of Selective Serotonin Reuptake Inhibitors (SSRI). (eurekaselect.com)
  • The serotonin-1A (5-HT1A) receptor is among the most abundant and widely distributed 5-HT receptors in the brain, but is also expressed on serotonin neurons as an autoreceptor where it plays a critical role in regulating the activity of the entire serotonin system. (biomedcentral.com)
  • In vivo recordings, however, suggest that unlike glutamatergic mitral cells, inhibitory granule cells are only weakly activated after sensory stimulation ( Cang and Isaacson, 2003 ). (jneurosci.org)
  • Proximal synapses arise from piriform cortical neurons and facilitate with paired-pulse stimulation, whereas distal dendrodendritic synapses generate EPSCs with slower kinetics that depress with paired stimulation. (jneurosci.org)
  • Elevated 5-HT1A autoreceptor expression would tend to reduce the activity of 5-HT neurons, while reduced post-synaptic 5-HT1A receptors would result in a blunted behavioral response to 5-HT. (biomedcentral.com)
  • Tetanic stimulation of axons in the granule cell layer (GCL) not only activates granule cells but also relieves the Mg blockade of NMDA receptors at distal dendrodendritic synapses ( Halabisky and Strowbridge, 2003 ). (jneurosci.org)
  • Taken together, these results highlight an integrated regulation of 5-HT1A autoreceptors that differs in several aspects from regulation of post-synaptic 5-HT1A receptors, and could be selectively targeted to enhance serotonergic neurotransmission. (biomedcentral.com)
  • Using two-photon guided minimal stimulation in acute rat brain slices, we found that distal and proximal excitatory synapses onto granule cells are functionally distinct. (jneurosci.org)
  • Over-expression of the 5-HT1A autoreceptor has been implicated in reducing serotonergic neurotransmission, and is associated with major depression and suicide. (biomedcentral.com)
  • Pet1, an obligatory enhancer for serotonergic differentiation, has been identified as a potent activator of 5-HT1A autoreceptor expression. (biomedcentral.com)
  • On the other hand, methiothepin is also unusual in getting able to markedly increase depolarization A 205804 clinical trial evoked pH]5 HT release at concentrations which will not modify basal release and this has been advised to reflect an inverse agonist action with the 5 HT terminal autoreceptor, a property quite possibly not shared by GRl27935. (gabasignaling.com)
  • van der Werf JF, Bast A, Bijloo GJ, Van der Vliet A, Timmerman H (1987) HA autoreceptor assay with superfused slices of rat brain cortex and electrical stimulation. (springer.com)
  • The discovery of extrasynaptic receptors by Miledi (1960) , was followed by observations by Dun and Minota (1982) of peripheral neuronal responses that could be attributed to somatic exocytosis of signaling molecules upon electrical stimulation. (frontiersin.org)
  • In view of the known loss of nigrostriatal dopamine neurons and decreases in striatal dopamine that occur with ageing, we predicted a decrement in apomorphine-induced yawning and penile grooming , responses that are thought to result from stimulation of autoreceptors located on dopamine nerve terminals. (baillement.com)
  • On the other hand, the results of receptor binding studies would predict decreased responsiveness to postsynaptic dopamine receptor stimulation in aged rats. (baillement.com)